US5427770A - Dentifrices containing amino alkyl silicones - Google Patents

Dentifrices containing amino alkyl silicones Download PDF

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US5427770A
US5427770A US08/004,489 US448993A US5427770A US 5427770 A US5427770 A US 5427770A US 448993 A US448993 A US 448993A US 5427770 A US5427770 A US 5427770A
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dentifrice
carbons
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John P. Viccaro
Samuel Lin
Todd Domke
Alexander G. Ziemkiewicz
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Chesebrough Ponds USA Inc
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
    • A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41—Amines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/43—Guanidines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/731—Cellulose; Quaternized cellulose derivatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/733—Alginic acid; Salts thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/90—Block copolymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses

Definitions

  • Staining can be troublesome, whether or not chlorhexidine is the cause.
  • the accumulation of stains on tooth surfaces poses an esthetic problem for many individuals.
  • Stains are usually extrinsic in nature and generally represent discolorations of the pellicle and/or plaque.
  • the exact mechanisms involved in stain formation are still obscure. It has been suggested that pigments produced by chromagenic bacteria, colored products from the chemical transformation of pellicle components and adsorption/retention of dietary constituents contribute to extrinsic stain formation.
  • the dietary factors which appear to contribute heavily to stain accumulation include coffee, tea, and red wines, as well as smoking.
  • staining is promoted by cationic antimicrobial agents such as hexetidine or quaternary ammonium compounds.
  • Plaque is a common factor in caries, gum disease and staining and greatly contributes to their development. Proper oral hygiene as currently practiced requires that plaque be removed or prevented not only for cosmetic purposes but also to eliminate a source of potential injury to teeth and gums.
  • Dental plaque is initiated when cariogenic bacteria adhere to pellicle, the proteinaceous film on the surface of teeth. These adherent bacteria metabolize dietary constituents, reproduce and accumulate to form the tenacious deposit known as, plaque.
  • Plaque generally consists of bacteria, bacterial end products such as polysaccharides, inorganic salts and salivary proteins. Plaque bacteria ferment dietary carbohydrates to organic acids which demineralize enamel, resulting in tooth decay.
  • Plaque acts as a nucleus for the formation of calculus (tartar) which is essentially plaque that has been mineralized with calcium phosphate salts. As calculus matures and hardens, it tends to stain noticeably due to adsorption of dietary chromagens: tea, coffee, smoke, etc. In addition to their unattractive appearance, calculus deposits, at the gum line, are a contributing source of gingivitis and periodontal disease.
  • Silicones have previously been suggested for inclusion in dentifrice compositions in that it has been expected that they would coat the teeth and thereby prevent cavities and staining.
  • British Patent Specification 689,679 discloses a mouthwash containing an organopolysiloxane for the purpose of preventing adhesion of, or for removal of, tars, stains, tartar and food particles from the teeth.
  • polymers such as those disclosed in the '679 specification, have not generally been successfully used for coating the teeth since it has been found that the polysiloxane does not adhere to the teeth for prolonged periods of time. Therefore, the need for dentifrice formulations including a hydrophobic substance which effectively coats the teeth has not been satisfied.
  • U.S. Pat. No. 3,624,120 discloses quaternary ammonium salts of cyclic siloxane polymers which are said to be useful as cationic surfactants, as bactericides and as anticariogenic agents. Yetter indicates that it is believed that the siloxane polymer absorbs on calcium phosphate to form a film which decreases the rate of acid solubilization. However, due to the solubility of the cyclic, surface active, low molecular weight, high N/Si ratio compounds of Yetter, it would not be expected that they could impart a lasting, strongly hydrophobic film to the surface of teeth.
  • dentifrices which include aminoalkyl silicones defined below form a hydrophobic barrier on the surface of teeth which is useful in preventing staining of teeth and in preventing cavities.
  • the antistaining properties of the dentifrices of the invention are of particular significance when the compounds of the invention are used in conjunction with antimicrobials such as quaternary salts or bis biguanides such as chlorhexidine.
  • the dentifrice provides the antistain and anticaries benefit of the aminoalkyl silicone together with the antibacterial and gum disease-fighting benefits of the quaternary ammonium salt or other antibacterial, without the usual disadvantage of staining.
  • the antistaining properties of the amino alkyl silicones may likewise be of use when other staining compounds such as stannous fluoride are included in the dentifrices.
  • the aminoalkyl silicones comprise amodimethicones. Also preferred are compounds having a molecular weight of about 5,000 and above and compounds which are non-cyclic.
  • aminoalkyl silicones included in the dentifrice of the invention comprise two basic units,
  • R 1 and R 2 are hydrocarbons or fluorinated hydrocarbons of 1 to 10 carbon atoms, hydroxy, alkoxy, hydrogen or acetoxy and R is ##STR1## wherein R 3 is a divalent alkylene of 1 to 20 carbons optionally including 0 atoms, R 4 , R 5 and R 6 may be different or the same and are selected from the group consisting of H, hydrocarbons of 1 to 20 carbons, and hydrocarbons of 1 to 20 carbons containing N and/or 0 atoms, preferably where the nitrogens are present as aliphatic amines and the oxygen atoms are present in hydroxyl groups, and X - is an anion preferably is selected from the group consisting of halide, hydroxide, tosylate and other monovalent anions.
  • the amino alkyl silicones of the invention include 60% or fewer, by repeat unit, of unit (1).
  • the aminoalkyl silicones of the invention may be linear, branched, random or block copolymers. Applicants have discovered that the above-defined aminoalkyl silicones when used in a dentifrice provide a hydrophobic film for the teeth which yields antistain and anticaries benefits.
  • the silicones of the invention have 60% or fewer repeat units of formula 1, more preferably 30% or fewer in order to combine acceptable substantivity of the film with modest cost and the absence of discoloration.
  • R 7 is a monovalent radical
  • R 8 is a divalent hydrocarbon radical
  • R 9 , R 10 , and R 11 may be the same or different and are selected from the group consisting of H, ##STR3## and R 12 , where R 12 is a monovalent hydrocarbon or hydrogen, and
  • R 13 and R 14 are the same or different monovalent radicals, a and c are integers selected from the group 0, 1, 2 and 3, and a plus c is 0, 1, 2 or 3, and
  • (II) an orally acceptable antimicrobial compound other than (I), such as chlorhexidine. It is preferred that 60% or fewer repeat units of Formula 3, preferably 30% or fewer, are present in the molecule.
  • the dentifrice of the invention can take several forms. It may, for instance, be a toothpaste cream or gel, or it may comprise a mouthwash; or it may be an oral spray, or chewing gum.
  • the aminofunctional silicone of the invention (whether amodimethicones or other amino alkyl silicones,) is present in the form of an emulsion.
  • an antimicrobial such as a quaternary ammonium salt or a bis biguanide such as chlorhexidine is included in the dentifrice together with the aminofunctional silicone.
  • Typical dentifrice ingredients may be included, depending, of course, on the form of the dentifrice.
  • Toothpastes and gels will generally include surfactant, one or more abrasives and may include humectants. Toothpastes also contain other components such as alcohol, water, flavor, etc. Mouthwashes will generally include alcohol, water and humectant. The dentifrice may also take the form of a denture cleaner.
  • mouthwashes are provided which include amino alkyl silicones and which can be formulated so as to be clear by matching the refractive index of the humectant and the amino alkyl silicone.
  • compositions of the invention may be useful in prevention of gum disease by reducing or preventing plaque. Indeed, as indicated above, plaque is a common factor in caries, gum disease and staining and greatly contributes to the development of each of these problems.
  • the positively charged nitrogen-containing silicones of the invention are attracted to negatively charges surfaces such as enamel so that silicones including alkyl amine groups are more substantive to the surface of the teeth.
  • increasing the number of aminoalkyl groups per molecule enhances the substantivity of the silicone.
  • the increased substantivity of aminoalkyl-containing silicones enables them to impart a durable water repellent barrier to enamel which is compatible with cationic antimicrobial/antiplaque agents.
  • Aminoalkyl silicones do not adversely affect the antiplaque activity of quats and/or bisbiquanides.
  • the aminoalkyl groups constitute from 5 to 30% by repeat unit of the polymer.
  • the number of silicon atoms which have nitrogen-containing moieties appended thereto constitute from 5 to 30% of the total number of silicon atoms.
  • the film of the alkylamino silicones of the invention will prevent the adhesion of staining materials such as chlorhexidine it is also believed that removal of such staining materials from the teeth will be facilitated thereby.
  • the dentifrices of the invention can reduce staining they would also provide a cosmetic as well as a health benefit.
  • the compositions of the invention will reduce pain and progression of root caries via the coating action and will reduce unpleasant tastes from dental product components such as antimicrobials and surfactants, and will prevent calculus growths.
  • coating of hypersensitive areas may result in desensitization, etc.
  • the aminoalkyl silicones of the invention may be incorporated into dentifrices as oils as well as emulsions, but preferably as emulsions.
  • the present invention also encompasses the process of applying the aminoalkyl silicones described herein onto the teeth, particularly in as an emulsion.
  • a preferred class of aminoalkyl silicone are the amodimethicones.
  • the dentifrices of the invention preferably contain from 0.1 to 2% by weight, even more preferably from 1% to 5% by weight of the aminoalkyl silicones of the invention.
  • the aminoalkyl silicones of the invention are non cyclic in general, and comprise two basic units of formulas 1 and 2 and may be linear, branched, random or block copolymers. Formulas 1 and 2 are as follows:
  • R 1 and R 2 are preferably hydrocarbons or fluorinated hydrocarbons of 1 to 10, even more preferably 1 to 4, carbon atoms. Examples include methyl, ethyl, phenyl, vinyl, trifluoropropyl and -cyanopropyl. Methyl and phenyl are preferred. R 1 and R 2 may also be hydroxyl, alkoxy, hydrogen, acetoxy or other reactive groups but their amounts are preferred to be low in order to promote adequate shelf stability.
  • R is defined as ##STR4## wherein R 3 is a divalent alkylene of 1 to 20 carbons optionally including 0 atoms, preferably 3 to 5 carbons.
  • R 4 , R 5 and R 6 may be different or the same and are H, hydrocarbons of 1 to 20 carbons, and hydrocarbons of 1 to 20 carbons containing N and/or 0 atoms.
  • R 4 , R 5 and R 6 preferably contain 1 to 10, even more preferably 1 to 4 carbon atoms. Examples are methyl, ethyl and phenyl.
  • X- is an anion preferably selected from the group consisting of halide, hydroxide, tosylate and other monovalent anions. Examples of R include: ##STR5##
  • the concentration of formula (1) in the aminoalkyl siloxane polymer may range from 1% to 99% by repeat units, preferably from 1 to 60%, more preferably from 5 to 30%, and even more preferably from 5 to 10%.
  • the preferred minimum molecular weight of the aminoalkyl silicone of the invention is 5,000. It is desirable that the molecular weight of the aminosilicones compounds be about 5,000 or greater since below 5,000 cyclization may occur and the compounds may dissolve in water. It is believed important that the silicones not be cyclized and not be soluble in order to permit them to deposit a lasting film onto the teeth. If the compounds are unduly soluble in water, it is believed that the film will too readily wash off the teeth.
  • the dentifrice preferably comprises a mixture including (I) from 0.01% to 20% by weight, even more preferably from 0.5% to 5% by weight of
  • an organosiloxane polymer which includes:
  • R 7 is a monovalent radical
  • R 8 is a divalent hydrocarbon radical
  • R 9 , R 10 , and R 11 may be the same or different and are selected from the group consisting of H, ##STR7## and R 12 , where R 12 is a monovalent hydrocarbon radical or hydrogen, and
  • R 13 and R 14 are the same or different monovalent radicals, a and c are integers selected from the group of 0, 1, 2 and 3 and a plus c is 0, 1, 2 or 3, and (II) from 0.001% to 3% more preferably from 0.1 to 1% by weight of an orally acceptable antibacterial compound, such as a quaternary ammonium compound other than (I) or a bis biguanide such as chlorhexidine.
  • an orally acceptable antibacterial compound such as a quaternary ammonium compound other than (I) or a bis biguanide such as chlorhexidine.
  • Each R 7 may independently be a hydrocarbon radical, a halogenated hydrocarbon radical, hydrogen, hydroxyl or alkenyl.
  • R 7 comprises from 1 to 10 and even 1 to 4 carbon atoms. Examples of R 7 are methyl, phenyl or -trifluoropropyl.
  • Each R 8 independently preferably comprises a divalent hydrocarbon radical having 3 or more carbons. Examples are propylene and butylene. Preferably R 8 does not exceed 10 carbon atoms.
  • R 12 is preferably selected from the group consisting of hydrogen, methyl or phenyl.
  • R 12 includes 10 or fewer carbon atoms, more preferably, 4 or fewer.
  • R 13 and R 14 are independently selected from the group consisting of hydrocarbon radicals, halogenated hydrocarbons, hydrogen, hydroxyl and alkoxyls. It is preferred that R 13 and R 14 include from 1 to 10, preferably from 1 to 4 carbon atoms. Especially preferred R 13 and R 14 groupings are independently selected from the group consisting of methyl, phenyl and -trifluoropropyl.
  • a plus c is equal to 2.
  • the preferred antibacterial compound is chlorhexidine.
  • Others include hexetidine, alexidine, quaternary ammonium antibacterial compounds and metal-ion containing antibacterial compounds mentioned later herein.
  • the "quats” usually include a quaternary ammonium group having at least one long chain of carbon atoms attached thereto.
  • the organopolysiloxane polymer comprising at least one unit of Formula 3 and one unit of Formula 4 may be used in a dentifrice according to the invention with or without the antibacterial compound.
  • the content of Formula 3 in the polymer ranges from 0.5% and up to 60% by repeat unit, preferably between 1 and 30%, more preferably from 5 to 15% by repeat unit.
  • the molecular weight is preferably above about 5,000.
  • the molecular weight of the preferred compound is preferably between 5,000 and 100,000, preferably between 5,000 and 30,000, although it may be as high as 1,000,000 or more.
  • An example of such a polysiloxane is as follows: ##STR9##
  • compositions in which the organosiloxane polymer has an average molecular weight in the ranges above are particularly preferred.
  • the silicones may be incorporated into dentifrices as silicone oils (and then emulsified in the dentifrice) or as silicone emulsions, preferably as emulsions.
  • Nonionic surfactants and/or cationic surfactants are preferred emulsifiers.
  • Certain cationic quaternary ammonium surfactants such as tallow trimethylammonium chloride and cetyl pyridinium chloride may be used to advantage in that they also deliver anti-plaque health benefits in addition to being emulsifiers.
  • the amines of the invention become protonated and bear positive charges when the pH is below their pKas.
  • the pKas will range from about 7 to about 12.
  • the pH of the dentifrices including the silicones of the invention should be below 10 and are preferably between 6 and 8 so that the aminoalkyl groups are protonated and degradation of the siloxane polymer is prevented.
  • the preferred dentifrices are toothpaste creams and gels, and mouthwashes.
  • Ingredients which may be included in toothpastes and gels generally and which may be used in toothpaste and gel compositions in accordance with the invention are abrasive polishing materials, sudsing agents, flavoring agents, humectants, binders, sweetening agents, alcohol and water.
  • Antitartar agents may be added to enhance the anticalculus affect of the present compositions.
  • Abrasives include alumina and hydrates thereof, such as alpha alumina trihydrate, magnesium trisilicate, magnesium carbonate, aluminosilicates, such as calcined aluminum silicate and aluminum silicate, calcium carbonate, zirconium silicate, polymethylmethacrylate, powdered polyethylene, silica and the like.
  • the abrasive may be present in an amount of from 0 to 70% by weight, preferably from 1 to 70%, more preferably from 10 to 70% for toothpastes.
  • Humectants contemplated for use in the present invention include glycerol, polyol, sorbitol, polyethylene glycols and propylene glycol.
  • the listed humectants are hydroxy functional compounds.
  • the humectants are generally present in amounts of from 0 to 80%, preferably from 1 to 70%, more preferably 5 to 70%, by weight.
  • Thickeners suitable for use in the invention include silica. Thickeners may be present in toothpaste creams and gels at 0.1 to 20% by weight.
  • Binders suitable for use in the dentifrice of the invention include hydroxy ethyl cellulose (Natrasol) and hydroxypropyl cellulose (Klucel).
  • Binders may be present in the toothpaste of the invention to the extent of from 0.01 to 3% by weight.
  • Alcohol is suitable for use in the present dentifrices, preferably at levels of about 0-5%, especially 0.5 to 5%, preferably 0.5 to 3%.
  • Certain pyrophosphate and other polyphosphate salts have been disclosed in U.S. Pat. Nos. 4,515,772 and 4,627,977 as being useful as antitartar agents. These include di- and tetra-alkali metal pyrophosphates wherein the alkali metals are preferably selected from the group consisting of sodium and potassium. Although phosphates are generally not favored as they tend to react with amino alkyl silicones, inclusion of these antitartar agents may be appropriate in certain formulations in accordance with our invention.
  • Zinc salts are disclosed as anticalculus agents in U.S. Pat. No. 4,100,269 and in U.S. Pat. Nos. 4,416,867, 4,425,325 and 4,339,432 (with glycine). These antitartar agents may be included in the present formulations.
  • surfactants used in the dentifrice of the invention be nonionic or cationic, although sarcosinate surfactants may be useful.
  • Surfactants include polyoxypropylene-polyoxyethylene block copolymer, sorbitan stearate, sorbitan oleate, polysorbates, nonoxynols, sodium cocoylsarcosinate, sodium lauryl sarcosinate dimethyl cocamine oxide, dimethyl lauryl amine oxide and monolauryl citrate esters.
  • Surfactants may be present within the range of 0 to 15%, preferably 0.1 to 15%, more preferably 0.25 to 10% by weight.
  • nonionic sudsing agents which may be suitable include condensation products of alkylene oxide groups with hydrophobic organic compounds such as alkyl phenols or the reaction products of propylene oxide and ethylene oxide diamine. Also included are the reaction products of ethylene oxide with aliphatic alcohols, long chain tertiary dialkyl sulfoxides.
  • the cationic surfactants may be quaternary ammonium compounds including one C 8 -C 18 alkyl chain. Examples include cetyl pyridinium chloride, cetyl trimethyl ammonium bromide, di isobutyl phenoxy ethoxy ethyl-dimethyl benzyl ammonium chloride and coconut alkyl trimethyl ammonium nitrate.
  • Hydrophilic silicones such as those sold under the name SILWETS by Union Carbide, may be used in the present formulations.
  • Flavors are usually included in dentifrices in low amounts of e.g., 0.10% to 3%. Any type of flavor may be used. However, low- and nonaldehydic flavors are generally preferred since the amines of the silicones may otherwise react with the acyl groups of the aldehyde to form Schiff bases, which are colored and which would make the nitrogen atoms on the silicones unavailable for interaction with the surface of the tooth.
  • Fluoride sources used in toothpastes such as sodium fluoride, stannous fluoride, zinc ammonium fluoride, tin ammonium fluoride, calcium fluoride and cobalt ammonium fluoride may be included.
  • Sodium monofluorophosphate may also be used, although it is not preferred as it tends to decrease deposition of the silicone. Since stannous fluoride tends to stain, its use together with the amino alkyl silicones of the invention may be particularly beneficial.
  • Fluoride ions are typically provided at a level of from 50 to 1500 ppm, although higher levels up to, say, 3000 ppm may be used in the present dentifrices.
  • Casein and its hydrolysate are other potential anticaries agents, e.g., at a level of 0.1 to 5% by weight.
  • Titanium dioxide is a suitable whitener.
  • Dyes/colorants suitable for dentifrices i.e. FD&C Blue #1, D&C Yellow #10, FD&C Red #40 etc. may be employed in the dentifrices of the invention.
  • mouthwashes comprise a water/alcohol solution, flavor, humectant, sweetener, sudsing agent, and colorant.
  • the corresponding compounds mentioned above which are used in toothpastes are generally suitable within the ranges above for mouthwashes as well.
  • the mouthwash can include ethanol at a level of from 0 to 30% preferably from 0.5 to 30%.
  • Nonionic and cationic surfactants are preferred.
  • the preferred clear mouthwashes of the invention comprise from 0.5 to 3% aminoalkylsilicone, preferably 1%, from 50 to 65% glycerol, preferably 50%, and from 0 to 2%. preferably 0.5 to 2%, more preferably 2%.
  • aminoalkylsilicone-containing formulations in which the refractive indexes of the ingredients are matched to form a clear mouthwash may be employed.
  • the amodimethicone of Formula 5 below is preferred.
  • the preferred concentration may range from 0.001% to 3%. Especially preferred concentrations range from 0.1% to 1%.
  • Cetylpyridinium chloride, phenolics such as DP300 ex Ciba Geigy and salicylamides (including salicylanilides), and sources of certain metal ions such as zinc, copper, silver and stannous (e.g., zinc, copper and stannous chloride, and silver nitrate) may also be appropriate antibacterial agents.
  • aminoalkylsilicone compounds are for the most part known. Methods of preparing aminoalkylsilicones are given in, for example, Jex et al., U.S. Pat. No. 2,930,809 including U.S. application Ser. Nos. 555,201 (filed Dec. 23, 1955), and 555,203 (Filed Dec. 23, 1955), all of which are hereby incorporated by reference.
  • the aminoalkyl polysiloxanes of the invention may be end capped. If end capped, one or more of the end capping groups, R e , preferably includes one or more nitrogen atoms.
  • R e may be --(CH 2 ) 3 NH 2 or --(CH 2 ) 3 NHCH 2 CH 2 NH 2 .
  • Amodimethicones are polydimethyl siloxane polymers containing aminoalkyl groups.
  • the aminoalkyl groups may be, for example, n-propylamine or n-propyl-N-ethylenediamine and these may be present either pendant or at one or more ends of the polydimethylsiloxane chain.
  • the amine groups cause the amodimethicone polymer to develop a net positive charge in aqueous systems over a wide range of pH say, from pH 1 to 10.
  • Examples of amodimethicones include Dow Corning's DC-929, DC-Q2-7224, and Q2-8075. These polymers comprise aminoalkyl groups affixed to a predominantly polydimethysiloxane structure.
  • the typical structure of Q2-8075's aminoalkyl group-containing units is: ##STR10##
  • a special class of aminosilicones are ethoxylated and propoxylated aminosilicone compounds such as the following ethoxylated compound: ##STR12## These have less of a tendency to react with aldehyde flavorants due to the presence of hydroxypropyl and hydroxyethyl groups. These compounds are described more fully in Lin et al. U.S. patent applications entitled “Dentifrices Including Modified Aminoalkyl Silicones", Ser. No. 07/276,719, filed Nov. 28, 1988, now U.S. Pat. No. 5,018,988 and "Hydroxylhydrocarbyl-modified Amino Alkyl Silicones", Ser. No. 07/276,726 filed Nov. 28, 1988, now abandoned, filed simultaneously herewith and incorporated by reference hereby.
  • Bovine incisors were cut, ground and polished so as to decrease enamel surface variables.
  • a standard area (approx. 40 mm 2 ) was masked off and the teeth were painted. Upon removal of the mask, the exposed enamel surfaces were brushed with a 0.5% Triton X-100 solution to remove residual adhesive. All the teeth were rinsed and stored in distilled, deionized water until treated.
  • Emulsions were prepared containing 35% of the respective silicone polymer (See Table 2) and 6.9% Tergitol NP-10. These were diluted with distilled water to yield a final concentration of 3% silicone oil. Treatments consisted of a 1 minute brushing and a 9 minute soaking in the 3% silicone emulsions followed by a 10 second rinse with distilled water.
  • Treated teeth were placed into a 0.1M lactic acid buffer, pH 4.5, at 37° C. and shaken at 200 rpm. Aliquots of the buffer were removed at different time intervals up to 30 minutes and assayed for phosphorus using the Chen assay for the microdetermination of phosphorus in accordance with "Official Methods of Analysis, Association of Official Analytical Chemists," edited by Sidney Williams, Arlington, Va. p. 632 Percent reductions in acid dissolution rate were calculated by comparing the silicone-treated teeth to a water treated control set. The results are set forth in Table 2.
  • the contact angle data of Example I showed amodimethicones to be more substantive to a pellicle-coated surface than dimethicones.
  • the acid dissolution data of the present example demonstrates the effectiveness of amino-functional silicones over alkyl silicones in depositing onto an enamel surface and in protecting it from caries.
  • amodimethicones Within the class of amodimethicones, it appears that those polymers having pendant alkylamines are more substantive to enamel and provide a better protective film than those having endcapping alkylamines. This increase in efficacy appears to be due to an overall increase in amine content (i.e., points for attachment). Indeed, the amodimethicones show a correlation between percent alkylamine and ability to reduce dissolution. Within the ranges of % alkylamine shown, an increase in alkylamine content tends to increase the % reduction in acid dissolution.
  • the methoxy group may further lend to the polymer's attachment to enamel through a covalent linkage thereby increasing polymer substantivity.
  • the DC-929 is a commercially available emulsion of a polyalkyl silicone having low pendant amine content and hydroxyl end groups. Hydroxyl end groups may also enhance deposition in a manner similar to that of the methoxyl groups.
  • aminoalkyl silicones are more substantive to enamel than dimethicones.
  • the most substantive amino silicone polymers are those which possess more than 3% alkylamine, pendantly attached to the polydimethylsiloxane backbone.
  • the rods were rinsed with sterile water to remove residual medium and then completely dried in vacuum over phosphorus pentoxide. Plaque accumulation was determined by dry weight measurements as follows: the dried plaque coated rods were weighed, stripped of plaque with a 1N NaOH. The rods were subsequently rinsed with water and acetone and thoroughly dried at 110° C. The dried rods were weighed and plaque weights determined by difference.
  • the treatments were aqueous solutions containing 25% human saliva supernatant and the following agents at the indicated concentrations: a) water control, b) 0.20% chlorhexidine, c) 0.20% chlorhexidine/3.0% amodimethicone, d) 0.25% chlorhexidine, e) 0.25% chlorhexidine/3.0% amodimethicone.
  • the amodimethicone employed was the compound of Formula 5 (page 20) which was emulsified with Tergitol surfactants and prepared as a 3.0% (w:v) emulsion.
  • amodimethicones offer the opportunity of reducing natural or dietary stains as well as stains produced by cationic antimicrobial agents.
  • the object of this study is to demonstrate the ability of amodimethicones to reduce stain on bovine teeth and hydroxyapatite disks caused by dietary chromagens, e.g. coffee, tea, etc.
  • Amodimethicone emulsions and an amodimethicone dentifrice were employed in the study.
  • Bovine Teeth Bovine incisors were cut into square slabs (approx. 1 cm 2 ) and mounted in acrylic plastic. The tooth surface was polished and its "whiteness" measured with a reflectometer. The enamel slabs were then placed into pooled human saliva and incubated at 36° C. for two hours, to form a pellicle on the tooth's surface. The teeth were rinsed with water, prior to treatment. Each slab was treated by brushing with a silicone emulsion for 30 seconds, followed by a 30 second soaking in the emulsion, rinsed with water and subsequently incubated in saliva for two hours at 36° C. This cycle of treatment and saliva soaking was repeated three times per day, ending with the slabs being incubated in saliva overnight. The following day the slabs were retreated three times as described above.
  • the treated slabs were stained by placing them in a tea/coffee solution for one minute, air dried, then soaked for one minute in ferrous ammonium sulfate solution, air dried, and ultimately immersed in human saliva for two hours at 36° C. This staining procedure was repeated seven times over a two day period. At the end of this period, the slabs were removed from the overnight soaking in saliva, air dried, and then lightly brushed with water (twenty strokes) to remove any loosely bound stain. All slabs were then air dried and their "whiteness" measured by a reflectometer. The difference in "whiteness" between the initial and final readings were employed to calculate percent stain reduction.
  • the solutions employed in the above Procedure were 3.0% (w:v) emulsions of: a) Union Carbide LE-460 HS, 28,000 MW dimethicone emulsion; and b) a 5,000 MW amodimethicone containing 10% alkylamine groups emulsified with a Tergitol surfactant.
  • Hydroxyapatite disks (29 mm diameter and 3 mm thickness) were prepared by pressing a mixture of hydroxyapatite powder and polyethylene powder (10%) in a hydraulic press. These disks were then heated at 110° C. overnight to enhance their firmness. The disks were submerged in the treatment silicone emulsions, brushed lightly for one minute, followed by a nine minute soaking period. The disks were then rinsed under running tap water and subsequently placed into a tea/coffee stain solution for one minute. Following this period, the disks were rinsed under running tap water, and during this rinsing the disks were lightly brushed until the stain was no longer removable.
  • the disks were air dried and their "color" measured by a reflectometer using the CIELAb color scale and D65 illumination.
  • the DE values obtained are a measure of the total color change as compared to a standard, in this case an unstained disk. As DE increases, so does the difference in color.
  • the treatment solutions utilized in the above experiment were 3.0% emulsions of: a) the compound of Formula 5 emulsified with Tergitol surfactants; b) Petrarch 1000 cst dimethicone (26,000 Mw) emulsified with Tergitol surfactants; c) Union Carbide dimethicone LE 460 HS emulsion (28,000 MW); d) Union Carbide LE 474 dimethicone emulsion (12,000 MW).
  • the dentifrice treatments were employed as slurries, prepared by adding two parts of water and one part dentifrice. Hydroxyapatite disks were treated with the dentifrice slurries as described above with the silicone emulsions.
  • the dentifrices used in this experiment were Topol, Colgate cream, Pepsodent and a silicone dentifrice containing 1.0% compound of Formula 5 (amodimethicone), alumina abrasive, gum thickener, surfactant, water, sorbitol liquid, saccharin and flavor.
  • amodimethicones are useful agents for preventing the staining of teeth caused by dietary chromagens, e.g. coffee and tea. Furthermore, amodimethicones displayed antistaining effects which were superior to those provided by dimethicones. Also, Table 5 shows that the antistaining qualities of an amodimethicone can be delivered from a dentifrice formulation.
  • hydroxyapatite powder was exposed in a pH 5 acetic acid solution which contained 5% silicone emulsion.
  • the powder (3.5%) was first treated with a 5% silicone emulsion (60-70 ml) for ten minutes, filtered, washed with distilled water, and then exposed to 150 ml acetic acid solution. Aliquots were withdrawn at various time intervals and the solution filtered to remove hydroxyapatite powder.
  • the experiment demonstrates that silicones decreased the rate of acid dissolution of hydroxyapatite powder and that the aminosilicones worked better than polydimethylsiloxane.
  • the untreated powder dissolved 348 ppm phosphate ion into the solution, but only 122 ppm when they were treated with aminosilicones, and 251 ppm when treated with polydimethylsiloxane.
  • the product was put on the rotary evaporator using vacuum first at room temperature and then heating to 85° C. for about an hour.
  • the Dean Stark condenser was used to remove the reaction by-products and solvents, and to drive the reaction to completion.
  • a rotary evaporator was used to remove the rest of the toluene.
  • a viscous slightly orange colored fluid was isolated as the product, (E).
  • a 60 MH z NMR spectrum was used to determine the amount of amine present in the cyclic product, to be 1.1 amine group (R 1 ) per D 3 unit (or D 4 1 .45R.spsp.1 in terms of D 4 for simplicity).
  • Toothpaste formulations were prepared by mixing the listed ingredients together. The toothpaste formulations were tested for reduction of acid dissolution as in Example 2. Results are given below.
  • Formula 5 refers to the formula on page 20 of the specification.
  • EO designates a compound which is ethoxylated in accordance with Lin et al. application entitled “Hydroxylhydrocarbyl-modified Aminoalkyl Silicones” filed simultaneously herewith mentioned above.
  • PPO refers to the propoxlated compound. Ethoxylation or propoxylation of an aminoalkyl silicone yields a compound in which the primary amines become bonded to two ⁇ hydroxy hydrocarbyl groups.
  • the mouthwash was made by dissolving 0.2% lauramine oxide in water. The amodimethicone was then added and emulsified. The emulsions thus prepared was added to glycerin and mixed. 0.1% lauramine oxide in ethanol was then dissolved in the mixture, flavor was added to ethanol and mixed, then added to the above mixture. The colors were added and mixed. Finally, chlorhexidine was added and mixed. A clear mouthwash resulted.
  • the mouthwash was prepared as follows:
  • Sorbitol and water were mixed.
  • the amodimethicone was emulsified with 0.09% tergitol and water and added to the sorbitol/water mixture. 0.30% tergitol was dissolved in ethanol and flavor was added. After mixing, the flavor mixture is added to the silicone emulsion. Colors were added and mixed. Finally, chlorhexidine was added and the preparation was mixed. A clear mouthwash was obtained.
  • lauramine oxide 0.2% lauramine oxide was dissolved in water. Amodimethicone was added and emulsified. The emulsions was added to glycerin and mixed. 0.1% lauramine oxide in ethanol was dissolved in the mixture. Flavor was added to ethanol and mixed, then added to the emulsion. Color was added and mixed. Chlorhexidine was added and mixed. A clear mouthwash was obtained.
  • Sorbitol and water were mixed together.
  • Amodimethicone was emulsified with 0.09% tergitol and 3.90% water and added to the sorbitol/water mixture and mixed.
  • 0.30% tergitol was dissolved in ethanol, after which flavor is added and the mixture is mixed.
  • the tergitol/ethanol/flavor was added to the emulsion after which colors were added and mixed. Finally, chlorhexidine was added and the preparation was mixed. A clear mouthwash resulted.

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US5611690A (en) * 1996-04-02 1997-03-18 E. Mishan & Sons, Inc. Method and apparatus for sprayed delivery of tooth bleaching agent
WO1998031298A1 (fr) * 1997-01-16 1998-07-23 The Procter & Gamble Company Procede pour le traitement des protheses dentaires
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Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB689679A (en) * 1950-12-11 1953-04-01 Dow Corning Ltd Improvements in or relating to mouthwash
US2806184A (en) * 1953-06-30 1957-09-10 Westinghouse Electric Corp Carrier relaying apparatus
US3032577A (en) * 1961-02-20 1962-05-01 Union Carbide Corp N-substituted derivatives of aminoalkylsiloxanes
US3389160A (en) * 1964-07-14 1968-06-18 Union Carbide Corp Dialkylamino hydroxy organosilicon compounds and derivatives thereof
US3402191A (en) * 1963-08-27 1968-09-17 Union Carbide Corp N, n-disubstituted aminoalkylsiloxane copolymers and amine oxide, quaternary ammonium salt, and coordination compounds of transition metal derivatives thereof
US3507955A (en) * 1968-11-25 1970-04-21 Prev Coat Corp Silicone containing dentifrices
GB1194885A (en) * 1967-06-16 1970-06-17 Prev Coat Corp Novel Silicone-Containing Dentifrices
US3544948A (en) * 1968-12-27 1970-12-01 Corning Glass Works Electroconductive coating resistor
US3597955A (en) * 1969-01-13 1971-08-10 Cyril Bath Co Apparatus for stretch drawing sheet stock under controlled tension
US3624120A (en) * 1969-12-22 1971-11-30 Procter & Gamble Quaternary ammonium salts of cyclic siloxane polymers
US3852075A (en) * 1973-10-16 1974-12-03 Procter & Gamble Hard surface rinse-coating composition and method
US3860709A (en) * 1971-09-29 1975-01-14 Dow Corning Method of inhibiting the growth of bacteria and fungi using organosilicon amines
GB1447254A (en) * 1973-08-16 1976-08-25 Ici Ltd Pharmaceutical compositions
US4071614A (en) * 1975-06-03 1978-01-31 Colgate Palmolive Company Dentifrice containing encapsulated flavoring
US4161518A (en) * 1977-12-29 1979-07-17 Minnesota Mining And Manufacturing Company Compositions and methods for inhibiting plaque formation
US4213961A (en) * 1978-03-23 1980-07-22 Beecham, Inc. Oral compositions
US4243658A (en) * 1979-04-02 1981-01-06 Minnesota Mining And Manufacturing Company Compositions and methods for reducing elution of therapeutic agents from teeth
US4246029A (en) * 1979-02-27 1981-01-20 Sws Silicones Corporation Detergent resistant vinyl coatings
US4256731A (en) * 1978-03-23 1981-03-17 Beecham, Inc. Oral Compositions
US4304766A (en) * 1979-04-02 1981-12-08 Minnesota Mining And Manufacturing Company Compositions for reducing elution of therapeutic agents from teeth
US4430235A (en) * 1981-07-17 1984-02-07 Union Carbide Corporation Polymeric antioxidants
US4450152A (en) * 1981-10-29 1984-05-22 Toray Silicone Company, Ltd. Composition used to groom hair
US4454110A (en) * 1982-05-24 1984-06-12 Forsyth Dental Infirmary For Children Self-gelling liquid composition for topical application in the oral cavity
US4485090A (en) * 1981-09-18 1984-11-27 Minnesota Mining And Manufacturing Company Composition and method for reducing elution of therapeutic agents from teeth
US4507455A (en) * 1984-05-11 1985-03-26 Dow Corning Corporation Silicones bearing acylated diaminohydrocarbyl radicals and method therefor
US4510127A (en) * 1981-09-18 1985-04-09 Minnesota Mining And Manufacturing Company Compositions and method for reducing elution of therapeutic agents from teeth
US4680366A (en) * 1985-06-20 1987-07-14 Shin-Etsu Chemical Co., Ltd. Fabric-finishing agent containing a novel organopolysiloxane
US5078988A (en) * 1988-11-28 1992-01-07 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Dentrifrices including modified aminoalkyl silicones
US5154915A (en) * 1988-11-28 1992-10-13 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Dentifrices containing aminoalkyl silicones and sarcosinate surfactants

Patent Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB689679A (en) * 1950-12-11 1953-04-01 Dow Corning Ltd Improvements in or relating to mouthwash
US2806184A (en) * 1953-06-30 1957-09-10 Westinghouse Electric Corp Carrier relaying apparatus
US3032577A (en) * 1961-02-20 1962-05-01 Union Carbide Corp N-substituted derivatives of aminoalkylsiloxanes
US3402191A (en) * 1963-08-27 1968-09-17 Union Carbide Corp N, n-disubstituted aminoalkylsiloxane copolymers and amine oxide, quaternary ammonium salt, and coordination compounds of transition metal derivatives thereof
US3389160A (en) * 1964-07-14 1968-06-18 Union Carbide Corp Dialkylamino hydroxy organosilicon compounds and derivatives thereof
GB1194885A (en) * 1967-06-16 1970-06-17 Prev Coat Corp Novel Silicone-Containing Dentifrices
US3507955A (en) * 1968-11-25 1970-04-21 Prev Coat Corp Silicone containing dentifrices
US3544948A (en) * 1968-12-27 1970-12-01 Corning Glass Works Electroconductive coating resistor
US3597955A (en) * 1969-01-13 1971-08-10 Cyril Bath Co Apparatus for stretch drawing sheet stock under controlled tension
US3624120A (en) * 1969-12-22 1971-11-30 Procter & Gamble Quaternary ammonium salts of cyclic siloxane polymers
US3860709A (en) * 1971-09-29 1975-01-14 Dow Corning Method of inhibiting the growth of bacteria and fungi using organosilicon amines
GB1447254A (en) * 1973-08-16 1976-08-25 Ici Ltd Pharmaceutical compositions
US3852075A (en) * 1973-10-16 1974-12-03 Procter & Gamble Hard surface rinse-coating composition and method
US4071614A (en) * 1975-06-03 1978-01-31 Colgate Palmolive Company Dentifrice containing encapsulated flavoring
US4161518A (en) * 1977-12-29 1979-07-17 Minnesota Mining And Manufacturing Company Compositions and methods for inhibiting plaque formation
US4256731A (en) * 1978-03-23 1981-03-17 Beecham, Inc. Oral Compositions
US4213961A (en) * 1978-03-23 1980-07-22 Beecham, Inc. Oral compositions
US4246029A (en) * 1979-02-27 1981-01-20 Sws Silicones Corporation Detergent resistant vinyl coatings
US4243658A (en) * 1979-04-02 1981-01-06 Minnesota Mining And Manufacturing Company Compositions and methods for reducing elution of therapeutic agents from teeth
US4304766A (en) * 1979-04-02 1981-12-08 Minnesota Mining And Manufacturing Company Compositions for reducing elution of therapeutic agents from teeth
US4430235A (en) * 1981-07-17 1984-02-07 Union Carbide Corporation Polymeric antioxidants
US4485090A (en) * 1981-09-18 1984-11-27 Minnesota Mining And Manufacturing Company Composition and method for reducing elution of therapeutic agents from teeth
US4510127A (en) * 1981-09-18 1985-04-09 Minnesota Mining And Manufacturing Company Compositions and method for reducing elution of therapeutic agents from teeth
US4450152A (en) * 1981-10-29 1984-05-22 Toray Silicone Company, Ltd. Composition used to groom hair
US4454110A (en) * 1982-05-24 1984-06-12 Forsyth Dental Infirmary For Children Self-gelling liquid composition for topical application in the oral cavity
US4507455A (en) * 1984-05-11 1985-03-26 Dow Corning Corporation Silicones bearing acylated diaminohydrocarbyl radicals and method therefor
US4680366A (en) * 1985-06-20 1987-07-14 Shin-Etsu Chemical Co., Ltd. Fabric-finishing agent containing a novel organopolysiloxane
US5078988A (en) * 1988-11-28 1992-01-07 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Dentrifrices including modified aminoalkyl silicones
US5154915A (en) * 1988-11-28 1992-10-13 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Dentifrices containing aminoalkyl silicones and sarcosinate surfactants

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
Chemical Abstracts; vol. 90; No. 16; 16 Apr. 1979, p. 612. *
European Search Report EP 89 20 2973. *
PCT Appln. WO79/ 00454. *
Seifen Ole Fette Wachse, vol. 114, No. 2, 4th Feb. 1988, Augsburg, De, pp. 51 54. *
Seifen-Ole-Fette-Wachse, vol. 114, No. 2, 4th Feb. 1988, Augsburg, De, pp. 51-54.

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WO1996019193A1 (fr) * 1994-12-22 1996-06-27 The Procter & Gamble Company Compositions a usage oral
WO1996019192A1 (fr) * 1994-12-22 1996-06-27 The Procter & Gamble Company Compositions a usage oral
US6153567A (en) * 1994-12-22 2000-11-28 The Procter & Gamble Company Silicone compositions
US6008171A (en) * 1994-12-22 1999-12-28 The Procter & Gamble Company Cleansing compositions
US6004538A (en) * 1995-04-28 1999-12-21 The Procter & Gamble Company Oral compositions
WO1997002011A1 (fr) * 1995-07-05 1997-01-23 The Procter & Gamble Company Compositions a usage buccal
US6193958B1 (en) * 1995-07-05 2001-02-27 The Procter & Gamble Company Oral compositions
WO1997036550A1 (fr) * 1996-04-02 1997-10-09 E. Mishan & Sons, Inc. Procede et appareil d'application par pulverisation d'un agent de blanchiment dentaire
US5611690A (en) * 1996-04-02 1997-03-18 E. Mishan & Sons, Inc. Method and apparatus for sprayed delivery of tooth bleaching agent
US6086373A (en) * 1996-07-25 2000-07-11 Schiff; Thomas Method of cleaning teeth with a toothbrush with improved cleaning and abrasion efficiency
WO1998031298A1 (fr) * 1997-01-16 1998-07-23 The Procter & Gamble Company Procede pour le traitement des protheses dentaires
US6217933B1 (en) 1997-01-16 2001-04-17 The Procter & Gamble Company Method for treating dentures
US6610149B2 (en) 1997-01-16 2003-08-26 The Procter & Gamble Company Apparatus for treating dentures
US20070269471A1 (en) * 1997-06-06 2007-11-22 The Procter & Gamble Company Methods of tooth bleaching
US20050238591A1 (en) * 1997-06-06 2005-10-27 Sagel Paul A Tooth whitening substances
WO2001001940A1 (fr) * 1999-07-02 2001-01-11 The Procter & Gamble Company Compositions comprenant des resines organosiloxanes, pour la liberation de substances d'hygiene buccale
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WO2001001958A1 (fr) * 1999-07-02 2001-01-11 The Procter & Gamble Company Systeme d'administration destine aux compositions de soins bucco-dentaires comprenant des resines d'organosiloxane utilisant une bandelette de soutien amovible
US6649147B1 (en) 1999-07-02 2003-11-18 The Procter & Gamble Company Delivery system for oral care compositions comprising organosiloxane resins using a removable backing strip
WO2001001939A1 (fr) * 1999-07-02 2001-01-11 The Procter & Gamble Company Compositions comprenant des resines organosiloxanes, pour la liberation de substances d'hygiene buccale
WO2001001942A1 (fr) * 1999-07-02 2001-01-11 The Procter & Gamble Company Systeme comprenant des resines d'organosiloxanes permettant d'administrer des substances destinees a l'hygiene buccale et de prolonger cette administration
USRE42126E1 (en) * 1999-07-02 2011-02-08 The Procter & Gamble Company Delivery system for oral care compositions comprising organosiloxane resins using a removable backing strip
AU769802B2 (en) * 1999-07-02 2004-02-05 Procter & Gamble Company, The Compositions comprising organosiloxane resins for delivering oral care substances
US6692727B1 (en) 1999-07-02 2004-02-17 The Procter & Gamble Company Systems comprising organosiloxane resins for delivering oral care substances and for prolonging such delivery
US20040146465A1 (en) * 2001-07-05 2004-07-29 Koichi Fujisawa Oral preparation
US7166272B2 (en) 2001-07-05 2007-01-23 Sunstar Inc. Oral preparation
US20030070319A1 (en) * 2001-10-16 2003-04-17 Minden Elizabeth Gaynor Pleatless ballet slipper
WO2003095559A1 (fr) 2002-05-09 2003-11-20 The Procter & Gamble Company Compositions comprenant des polyorganosiloxanes fonctionnalises anioniques afin de modifier des surfaces sur le plan hydrophobe et d'ameliorer l'apport d'agents actifs aux surfaces traitees a l'aide de ces compositions
US7025950B2 (en) 2002-05-09 2006-04-11 The Procter & Gamble Company Oral care compositions comprising dicarboxy functionalized polyorganosiloxanes
US7166235B2 (en) 2002-05-09 2007-01-23 The Procter & Gamble Company Compositions comprising anionic functionalized polyorganosiloxanes for hydrophobically modifying surfaces and enhancing delivery of active agents to surfaces treated therewith
US20040019990A1 (en) * 2002-08-01 2004-02-05 Farrell Lawrence W. Enhanced dental hygiene system with direct UVA photoexcitation
US6902397B2 (en) 2002-08-01 2005-06-07 Sunstar Americas, Inc. Enhanced dental hygiene system with direct UVA photoexcitation
US10493016B2 (en) 2002-09-11 2019-12-03 The Procter & Gamble Company Tooth whitening product
US9554976B2 (en) 2002-09-11 2017-01-31 The Procter & Gamble Company Tooth whitening product
US20040166068A1 (en) * 2003-02-20 2004-08-26 The Procter & Gamble Company Antiplaque denture adhesive compositions
US7118732B2 (en) * 2004-05-10 2006-10-10 Colgate-Palmolive Company Tooth-whitening compositions comprising silicone polymer and methods therefor
US20050287084A1 (en) * 2004-05-10 2005-12-29 Sayed Ibrahim Tooth-whitening compositions comprising silicone polymer and methods therefor
US20060140881A1 (en) * 2004-12-22 2006-06-29 Guofeng Xu Oral care compositions containing flavonoids and flavans
US20070280893A1 (en) * 2006-06-05 2007-12-06 Betafarma S.P.A Antibacterial composition to be used as a toothpaste for sanitating the oral cavity
US10285916B2 (en) 2012-10-17 2019-05-14 The Procter & Gamble Company Strip for the delivery of an oral care active and methods for applying oral care actives
US10285915B2 (en) 2012-10-17 2019-05-14 The Procter & Gamble Company Strip for the delivery of an oral care active and methods for applying oral care actives
US20150023892A1 (en) * 2013-07-16 2015-01-22 Nian Wu Mouth wash compositions for denture adhesive removal
CN107028813A (zh) * 2017-04-18 2017-08-11 新疆中草堂医药科技有限公司 紫苏精油在制备口腔护理品中的应用

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DE68904539D1 (de) 1993-03-04
EP0373688A2 (fr) 1990-06-20
ES2053962T3 (es) 1994-08-01
DE68904539T2 (de) 1993-06-03
JPH0561248B2 (fr) 1993-09-06
EP0373688B1 (fr) 1993-01-20
EP0373688A3 (en) 1990-06-27
CA2003969A1 (fr) 1990-05-28
JPH02223512A (ja) 1990-09-05

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